CILIARY DYSKINESIA, PRIMARY, 21
|
disease |
|
Disease or Syndrome
|
1
|
2
|
0.800 |
None |
|
0 |
2
|
|
|
Congenital atresia of nasopharynx
|
disease |
Stomatognathic Diseases; Otorhinolaryngologic Diseases
|
Congenital Abnormality
|
13
|
|
0.200 |
None |
|
0 |
|
|
|
Other specified congenital malformations of respiratory system
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
|
Congenital Abnormality
|
13
|
|
0.200 |
None |
|
0 |
|
|
|
Heterotaxy, Visceral, 3, Autosomal
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
29
|
|
0.200 |
None |
|
0 |
|
|
|
HETEROTAXY, VISCERAL, 4, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
29
|
2
|
0.200 |
None |
|
0 |
|
|
|
HETEROTAXY, VISCERAL, 1, X-LINKED
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
30
|
17
|
0.200 |
None |
|
0 |
|
|
|
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
|
disease |
|
Disease or Syndrome
|
30
|
3
|
0.200 |
None |
|
0 |
|
|
|
HETEROTAXY, VISCERAL, 6, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
30
|
2
|
0.200 |
None |
|
0 |
|
|
|
Rothmund-Thomson syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
35
|
12
|
0.010 |
None |
1.000 |
1 |
|
2005 |
2005 |
Polynesian Bronchiectasis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
35
|
|
0.500 |
None |
1.000 |
1 |
|
2013 |
2013 |
HETEROTAXY, VISCERAL, 2, AUTOSOMAL
|
disease |
|
Disease or Syndrome
|
39
|
5
|
0.200 |
None |
|
0 |
|
|
|
Heterotaxy Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
39
|
8
|
0.200 |
None |
|
0 |
|
|
|
Immotile cilia
|
phenotype |
|
Finding
|
41
|
|
0.100 |
None |
|
0 |
|
|
|
Impaired nasal mucociliary clearance
|
phenotype |
|
Finding
|
41
|
|
0.100 |
None |
|
0 |
|
|
|
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
43
|
67
|
0.700 |
moderate |
1.000 |
1 |
2
|
2013 |
2013 |
Halitosis
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Sign or Symptom
|
48
|
|
0.100 |
None |
|
0 |
|
|
|
Ectopic Pregnancy
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications
|
Pathologic Function
|
48
|
|
0.100 |
None |
|
0 |
|
|
|
Ciliary Motility Disorders
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
|
Disease or Syndrome
|
59
|
402
|
0.100 |
None |
1.000 |
1 |
3
|
2013 |
2013 |
Atelectasis
|
phenotype |
Respiratory Tract Diseases
|
Pathologic Function
|
62
|
2
|
0.100 |
None |
|
0 |
|
|
|
Kartagener Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases
|
Disease or Syndrome
|
67
|
3
|
0.710 |
None |
1.000 |
2 |
|
2013 |
2019 |
Congenital absence of spleen
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Hemic and Lymphatic Diseases
|
Congenital Abnormality
|
80
|
6
|
0.100 |
None |
|
0 |
|
|
|
Tachypnea
|
phenotype |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
|
Finding
|
82
|
5
|
0.100 |
None |
|
0 |
|
|
|
Clubbed Fingers
|
disease |
Musculoskeletal Diseases
|
Anatomical Abnormality
|
88
|
1
|
0.100 |
None |
|
0 |
|
|
|
Lung Diseases, Obstructive
|
group |
Respiratory Tract Diseases
|
Disease or Syndrome
|
104
|
4
|
0.100 |
None |
|
0 |
|
|
|
Situs inversus totalis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
104
|
8
|
0.100 |
None |
|
0 |
|
|
|